Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP542727.RAXpJB2UOg9085uVOLSXtwdQ8w4VKKxVZjt1TKa2wi8Bw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP542727.RAXpJB2UOg9085uVOLSXtwdQ8w4VKKxVZjt1TKa2wi8Bw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP542727.RAXpJB2UOg9085uVOLSXtwdQ8w4VKKxVZjt1TKa2wi8Bw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP542727.RAXpJB2UOg9085uVOLSXtwdQ8w4VKKxVZjt1TKa2wi8Bw130_provenance.
- NP542727.RAXpJB2UOg9085uVOLSXtwdQ8w4VKKxVZjt1TKa2wi8Bw130_assertion description "[WDR35 is homologous to TULP4 (from the Tubby superfamily) and has previously been characterized as an intraflagellar transport component, confirming that Sensenbrenner syndrome is a ciliary disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP542727.RAXpJB2UOg9085uVOLSXtwdQ8w4VKKxVZjt1TKa2wi8Bw130_provenance.
- NP542727.RAXpJB2UOg9085uVOLSXtwdQ8w4VKKxVZjt1TKa2wi8Bw130_assertion evidence source_evidence_literature NP542727.RAXpJB2UOg9085uVOLSXtwdQ8w4VKKxVZjt1TKa2wi8Bw130_provenance.
- NP542727.RAXpJB2UOg9085uVOLSXtwdQ8w4VKKxVZjt1TKa2wi8Bw130_assertion SIO_000772 20817137 NP542727.RAXpJB2UOg9085uVOLSXtwdQ8w4VKKxVZjt1TKa2wi8Bw130_provenance.
- NP542727.RAXpJB2UOg9085uVOLSXtwdQ8w4VKKxVZjt1TKa2wi8Bw130_assertion wasDerivedFrom befree-20140225 NP542727.RAXpJB2UOg9085uVOLSXtwdQ8w4VKKxVZjt1TKa2wi8Bw130_provenance.
- NP542727.RAXpJB2UOg9085uVOLSXtwdQ8w4VKKxVZjt1TKa2wi8Bw130_assertion wasGeneratedBy ECO_0000203 NP542727.RAXpJB2UOg9085uVOLSXtwdQ8w4VKKxVZjt1TKa2wi8Bw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP542727.RAXpJB2UOg9085uVOLSXtwdQ8w4VKKxVZjt1TKa2wi8Bw130_provenance.